Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:48830969-48831252 | Rare:81 | ||||
chr4:52659192-52659439 | Common:1; Rare:82 | ||||
chr4:53365997-53366222 | Rare:52 | ||||
chr4:54657695-54657971 | Common:2; Rare:96 | ||||
chr4:56387428-56387534 | Rare:37 | ||||
chr4:56435551-56435759 | Common:3; Rare:70 | ||||
chr4:56436012-56436307 | Rare:105 | ||||
chr4:56467520-56467687 | Common:2; Rare:69; Clinvar (benign):4 | ||||
chr4:56656345-56656567 | Common:3; Rare:34 | ||||
chr4:56977603-56977753 | Common:1; Rare:51 | ||||
chr4:67545377-67545742 | Common:2; Rare:87 | ||||
chr4:67701117-67701371 | Common:4; Rare:119 | ||||
chr4:70688433-70688579 | Common:2; Rare:39 | ||||
chr4:70839232-70839419 | Common:2; Rare:80 | ||||
chr4:70902174-70902402 | Common:5; Rare:81 |